JP2011528730A5 - - Google Patents
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- JP2011528730A5 JP2011528730A5 JP2011518929A JP2011518929A JP2011528730A5 JP 2011528730 A5 JP2011528730 A5 JP 2011528730A5 JP 2011518929 A JP2011518929 A JP 2011518929A JP 2011518929 A JP2011518929 A JP 2011518929A JP 2011528730 A5 JP2011528730 A5 JP 2011528730A5
- Authority
- JP
- Japan
- Prior art keywords
- polyolefin
- terminated
- allyl
- copolymer
- molecular weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 229920000098 polyolefin Polymers 0.000 claims 21
- 229920001577 copolymer Polymers 0.000 claims 14
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 5
- -1 allylsilane compound Chemical class 0.000 claims 5
- 238000006116 polymerization reaction Methods 0.000 claims 5
- 230000002378 acidificating Effects 0.000 claims 4
- 239000003999 initiator Substances 0.000 claims 4
- 239000000376 reactant Substances 0.000 claims 4
- 239000002841 Lewis acid Substances 0.000 claims 3
- 150000007517 lewis acids Chemical class 0.000 claims 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- HYWCXWRMUZYRPH-UHFFFAOYSA-N trimethyl(prop-2-enyl)silane Chemical compound C[Si](C)(C)CC=C HYWCXWRMUZYRPH-UHFFFAOYSA-N 0.000 claims 2
- 229920002367 Polyisobutene Polymers 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 238000010550 living polymerization reaction Methods 0.000 claims 1
- 230000001050 lubricating Effects 0.000 claims 1
- 239000010687 lubricating oil Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- 229920000768 polyamine Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000001384 succinic acid Substances 0.000 claims 1
Claims (15)
(a)ポリオレフィンをイオン化して炭素カチオン末端ポリオレフィンを生成させる、
(b)工程(a)の炭素カチオン末端ポリオレフィンをルイス酸の存在下でアリルシラン化合物と反応させ、そして
(c)工程(b)を終結させてアリル末端重合生成物を生成させることにより製造されるアリル末端重合生成物であるか;あるいは、
(ii)アリル末端重合生成物が、
(a)ルイス酸の存在下かつ適切な準リビング条件下で準リビング3級ハロゲン化末端ポリオレフィンを生成させ、
(b)該準リビング3級ハロゲン化末端ポリオレフィンをアリルシラン化合物と反応させ、そして
(c)工程(b)を終結させてアリル末端準リビング重合生成物を生成させることにより製造されるアリル末端準リビング重合生成物である請求項1の共重合体。 (I) an allyl-terminated polymerization product
(A) ionizing the polyolefin to produce a carbocation terminated polyolefin;
(B) produced by reacting the carbocation terminated polyolefin of step (a) with an allylsilane compound in the presence of a Lewis acid, and (c) terminating step (b) to produce an allyl terminated polymer product. An allyl-terminated polymerization product; or
(Ii) the allyl-terminated polymerization product is
(A) producing a quasi-living tertiary halogenated terminal polyolefin in the presence of a Lewis acid and under suitable quasi-living conditions;
(B) an allyl-terminated quasi-living produced by reacting the quasi-living tertiary halogenated terminal polyolefin with an allylsilane compound, and (c) terminating step (b) to produce an allyl-terminated quasi-living polymerization product. The copolymer of claim 1 which is a polymerization product.
(ii)共重合体が1乃至2、もしくは1.0乃至1.5のコハク酸比を有するか;
(iii)ポリオレフィンが少なくとも75%、もしくは少なくとも90%のアリル末端基の含有率を有するか;あるいは
(iv)ポリオレフィンが2未満、もしくは1.4未満の分散指数を有するかである請求項1乃至4のうちのいずれか一項に記載の共重合体。 (I) whether the polyolefin has a number average molecular weight of 500 to 10,000, or 900 to 5,000;
(Ii) the copolymer has a succinic acid ratio of 1 to 2, or 1.0 to 1.5;
(Iii) a polyolefin of at least 75%, or either with a content of at least 90% of the allyl end groups; 1 to claim is or having or (iv) dispersion index of the polyolefin is less than 2, or less than 1.4 5. The copolymer according to any one of 4 .
(a)高分子量のアリル末端ポリオレフィンを生成させる;そして
(b)該アリル末端ポリオレフィンを、フリーラジカル開始剤の存在下で不飽和酸性反応体と接触させて共重合体を生成させる。 A method for producing a copolymer comprising:
(A) producing a high molecular weight allyl-terminated polyolefin; and (b) contacting the allyl-terminated polyolefin with an unsaturated acidic reactant in the presence of a free radical initiator to produce a copolymer.
(a)ポリオレフィンをイオン化して炭素カチオン末端ポリオレフィンを生成させ、
(b)工程(a)の炭素カチオン末端ポリオレフィンをルイス酸の存在下でアリルシラン化合物と反応させ、そして
(c)工程(b)を終結させてアリル末端ポリオレフィンを生成させる。 12. The method of claim 11, wherein the allyl terminated polyolefin is produced by the following steps:
(A) ionizing the polyolefin to produce a carbocation terminated polyolefin;
(B) reacting the carbocation terminated polyolefin of step (a) with an allylsilane compound in the presence of a Lewis acid, and (c) terminating step (b) to form an allyl terminated polyolefin.
(ii)ポリオレフィンが少なくとも75%、もしくは少なくとも90%のアリル末端基の含有率を有する
上記請求項11乃至13のうちのいずれか一項に記載の方法。 14. (i) The polyolefin has a number average molecular weight of 500 to 10,000, or 900 to 5000; or (ii) the polyolefin has an allyl end group content of at least 75%, or at least 90%. The method according to any one of the above .
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/176,292 US20100016191A1 (en) | 2008-07-18 | 2008-07-18 | Copolymers Made With Allyl-Terminated Polyolefins And Unsaturated Acidic Reagents, Dispersants Using Same, and Methods of Making Same |
US12/176,292 | 2008-07-18 | ||
PCT/US2009/050965 WO2010009379A2 (en) | 2008-07-18 | 2009-07-17 | Copolymers made with allyl-terminated polyolefins and unsaturated acidic reagents, dispersants using same, and methods of making same |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2011528730A JP2011528730A (en) | 2011-11-24 |
JP2011528730A5 true JP2011528730A5 (en) | 2012-08-30 |
JP5806614B2 JP5806614B2 (en) | 2015-11-10 |
Family
ID=41530811
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011518929A Active JP5806614B2 (en) | 2008-07-18 | 2009-07-17 | Copolymer produced from allyl-terminated polyolefin and unsaturated acidic reagent, dispersant using the same, and method for producing the same |
Country Status (6)
Country | Link |
---|---|
US (2) | US20100016191A1 (en) |
EP (1) | EP2303939B1 (en) |
JP (1) | JP5806614B2 (en) |
CN (1) | CN102099389B (en) |
CA (1) | CA2730127C (en) |
WO (1) | WO2010009379A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8344073B2 (en) * | 2009-01-16 | 2013-01-01 | The University Of Southern Mississippi | Functionalization of polyolefins with phenoxy derivatives |
KR101781668B1 (en) * | 2010-09-07 | 2017-10-23 | 바스프 에스이 | Terpolymer formed from electron-deficient olefins, olefins without electron-withdrawing substituents and alkoxyvinylsilanes |
ES2526528T3 (en) * | 2011-01-18 | 2015-01-13 | Basf Se | Hydrolysis stable polyamides |
US9243203B2 (en) * | 2012-11-30 | 2016-01-26 | Chevron Oronite Company Llc | Copolymers of polyaminopolyolefins and polyanhydrides and methods of their preparation |
CN105745230B (en) | 2013-11-27 | 2019-08-13 | 日本瑞翁株式会社 | The manufacturing method of radical polymerization initiator and polymer |
WO2024030592A1 (en) * | 2022-08-05 | 2024-02-08 | The Lubrizol Corporation | Processes for producing radically-functionalized pibsa product derivatives and compositions comprising same |
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US4034038A (en) * | 1963-11-13 | 1977-07-05 | The Lubrizol Corporation | Boron-containing esters |
US4276394A (en) * | 1979-09-10 | 1981-06-30 | The University Of Akron | Novel telechelic polymers, block copolymers and processes for the preparation thereof |
US4568732A (en) * | 1985-01-09 | 1986-02-04 | The University Of Akron | Continuous telechelic polymer process |
JPH0811763B2 (en) * | 1985-06-10 | 1996-02-07 | 日本ゼオン株式会社 | α, β-Unsaturated dicarboxylic acid anhydride polymer |
CA1338541C (en) | 1985-06-20 | 1996-08-20 | Joseph P. Kennedy | Living catalysts, complexes and polymers therefrom |
US4758631A (en) * | 1986-10-16 | 1988-07-19 | Dow Corning Corporation | Method of preparing allyl-terminated polyisobutylene |
EP0268214B1 (en) * | 1986-11-13 | 1991-08-21 | Idemitsu Kosan Company Limited | Process for producing propylene oligomers |
JP2653067B2 (en) * | 1987-06-12 | 1997-09-10 | 三菱化学株式会社 | Method for producing α-olefin-maleic anhydride copolymer |
US5112507A (en) * | 1988-09-29 | 1992-05-12 | Chevron Research And Technology Company | Polymeric dispersants having alternating polyalkylene and succinic groups |
US5175225A (en) * | 1989-09-29 | 1992-12-29 | Chevron Research And Technology Company | Process for preparing polymeric dispersants having alternating polyalkylene and succinic groups |
US5334321A (en) * | 1993-03-09 | 1994-08-02 | Chevron Research And Technology Company, A Division Of Chevron U.S.A. Inc. | Modified high molecular weight succinimides |
JP3001385B2 (en) * | 1993-12-13 | 2000-01-24 | シェブロン ケミカル カンパニー | Polymer dispersant |
US5528108A (en) | 1994-09-22 | 1996-06-18 | Motorola | Field emission device arc-suppressor |
US5616153A (en) * | 1995-10-03 | 1997-04-01 | Ethyl Corporation | Copolymer dispersants via vinyl terminated propene polymers |
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US6100224A (en) * | 1997-10-01 | 2000-08-08 | Exxon Chemical Patents Inc | Copolymers of ethylene α-olefin macromers and dicarboxylic monomers and derivatives thereof, useful as additives in lubricating oils and in fuels |
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US6906011B2 (en) * | 2001-11-09 | 2005-06-14 | Chevron Oronite Company Llc | Polymeric dispersants prepared from copolymers of low molecular weight polyisobutene and unsaturated acidic reagent |
DE10162567A1 (en) * | 2001-12-19 | 2003-07-03 | Basf Ag | Polyisobutenes and polyisobutene derivatives for lubricant compositions |
US6969744B2 (en) * | 2003-06-19 | 2005-11-29 | University Of Southern Mississippi | Living and quasiliving cationic telechelic polymers quenched by N-substituted pyrrole and methods for their preparation |
EP2284203B1 (en) * | 2004-08-20 | 2015-03-04 | Chevron Oronite Company LLC | Method for preparation of polyolefins containing exo-olefin chain ends |
CA2577728C (en) * | 2004-08-20 | 2014-10-14 | Chevron Oronite Company Llc | Method for preparation of polyolefins containing exo-olefin chain ends |
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WO2006110647A1 (en) | 2005-04-08 | 2006-10-19 | University Of Massachusetts Lowell Research Foundation | Capping reactions in cationic polymerization; kinetic and synthetic utility |
US7816459B2 (en) * | 2005-12-30 | 2010-10-19 | Chevron Oronite Company Llc | Method for preparing polyolefins containing vinylidine end groups using polymeric nitrogen compounds |
US8013073B2 (en) * | 2005-12-30 | 2011-09-06 | Chevron Oronite Company Llc | Method for preparing polyolefins containing vinylidine end groups using nonaromatic heterocyclic compounds |
US7501476B2 (en) * | 2005-12-30 | 2009-03-10 | Chevron Oronite Company, Llc | Method for preparing polyolefins containing vinylidene end groups using azole compounds |
US9818088B2 (en) | 2011-04-22 | 2017-11-14 | Emerging Automotive, Llc | Vehicles and cloud systems for providing recommendations to vehicle users to handle alerts associated with the vehicle |
-
2008
- 2008-07-18 US US12/176,292 patent/US20100016191A1/en not_active Abandoned
-
2009
- 2009-07-17 CA CA2730127A patent/CA2730127C/en active Active
- 2009-07-17 WO PCT/US2009/050965 patent/WO2010009379A2/en active Application Filing
- 2009-07-17 CN CN2009801278717A patent/CN102099389B/en active Active
- 2009-07-17 JP JP2011518929A patent/JP5806614B2/en active Active
- 2009-07-17 EP EP09798796.0A patent/EP2303939B1/en active Active
-
2015
- 2015-10-14 US US14/883,519 patent/US20160032041A1/en not_active Abandoned
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